Evidence map›Paper›PMID 35188589›Full record

ArticleBrain structure & function2022

Differential distribution of inhibitory neuron types in subregions of claustrum and dorsal endopiriform nucleus of the short-tailed fruit bat.

Timothy Morello, Richard Kollmar, Abdessamad Ramzaoui, Mark Stewart, Rena Orman

Abstract read
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In one paragraph

Article in Brain structure & function, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Bats as instructive animal models for studying longevity and aging.Annals of the New York Academy of Sciences · 2024
    Review
  4. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Timothy MorelloDepartment of Physiology and Pharmacology, SUNY Downstate Health Sciences University, 450 Clarkson Avenue, MSC 31, Brooklyn, NY, 11203, USA.
Richard KollmarDepartment of Cell Biology, SUNY Downstate Health Sciences University, Brooklyn, NY, USA.
Abdessamad RamzaouiCUNY Kingsborough Community College, Brooklyn, NY, USA.
Mark StewartDepartment of Physiology and Pharmacology, SUNY Downstate Health Sciences University, 450 Clarkson Avenue, MSC 31, Brooklyn, NY, 11203, USA.
Rena OrmanDepartment of Physiology and Pharmacology, SUNY Downstate Health Sciences University, 450 Clarkson Avenue, MSC 31, Brooklyn, NY, 11203, USA. rena.orman@downstate.edu.
SUNY Downstate Health Sciences University · USKingsborough Community College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Few brain regions have such wide-ranging inputs and outputs as the claustrum does, and fewer have posed equivalent challenges in defining their structural boundaries. We studied the distributions of three calcium-binding proteins-calretinin, parvalbumin, and calbindin-in the claustrum and dorsal endopiriform nucleus of the fruit bat, Carollia perspicillata. The proportionately large sizes of claustrum and dorsal endopiriform nucleus in Carollia brain afford unique access to these structures' intrinsic anatomy. Latexin immunoreactivity permits a separation of claustrum into core and shell subregions and an equivalent separation of dorsal endopiriform nucleus. Using latexin labeling, we found that the claustral shell in Carollia brain can be further subdivided into at least four distinct subregions. Calretinin and parvalbumin immunoreactivity reinforced the boundaries of the claustral core and its shell subregions with diametrically opposite distribution patterns. Calretinin, parvalbumin, and calbindin all colocalized with GAD67, indicating that these proteins label inhibitory neurons in both claustrum and dorsal endopiriform nucleus. Calretinin, however, also colocalized with latexin in a subset of neurons. Confocal microscopy revealed appositions that suggest synaptic contacts between cells labeled for each of the three calcium-binding proteins and latexin-immunoreactive somata in claustrum and dorsal endopiriform nucleus. Our results indicate significant subregional differences in the intrinsic inhibitory connectivity within and between claustrum and dorsal endopiriform nucleus. We conclude that the claustrum is structurally more complex than previously appreciated and that claustral and dorsal endopiriform nucleus subregions are differentially modulated by multiple inhibitory systems. These findings can also account for the excitability differences between claustrum and dorsal endopiriform nucleus described previously.

Indexed as

ChiropteraClaustrumAnimalsBasal GangliaCalbindin 2CalbindinsCalcium-Binding ProteinsNeuronsParvalbuminsS100 Calcium Binding Protein GCalbindin 2CalbindinsCalcium-Binding ProteinsParvalbuminsS100 Calcium Binding Protein GCalbindinCalcium-binding proteinsCalretininCarollia perspicillataGAD67LatexinParvalbumin

Identifiers

PMID35188589
OpenAlexW4213267438

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.